{{Rsnum
|rsid=386134172
|Chromosome=19
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PRKCG
|position=53906729
|Gene_s=PRKCG
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=19
|CLNACC=RCV000034969.1
|CLNALLE=1
|CLNDBN=Spinocerebellar ataxia 14
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1399:C1854369:605361:98763
|CLNHGVS=NC_000019.9:g.54409983T>C
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1399
|Disease=Spinocerebellar ataxia 14
|FwdALT=C
|FwdREF=T
|REF=T
|RSPOS=54409983
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;SLO;NSM;REF;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000a00000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=386134172
}}{{PMID Auto
|PMID=15313841
|Title=Mutation in the catalytic domain of protein kinase C gamma and extension of the phenotype associated with spinocerebellar ataxia type 14.
}}

{{PMID Auto
|PMID=16193476
|Title=New mutations in protein kinase Cgamma associated with spinocerebellar ataxia type 14.
}}